Literature DB >> 33935496

Magnetic Fluid Hyperthermia as Treatment Option for Pancreatic Cancer Cells and Pancreatic Cancer Organoids.

Julian Palzer1,2, Benedikt Mues2, Richard Goerg1,2, Merel Aberle3, Sander S Rensen3, Steven W M Olde Damink1,3, Rianne D W Vaes3, Thorsten Cramer1,3, Thomas Schmitz-Rode2, Ulf P Neumann1,3, Ioana Slabu2, Anjali A Roeth1,3.   

Abstract

INTRODUCTION: Pancreatic ductal adenocarcinoma (PDAC) is a cancer with a meager prognosis due to its chemotherapy resistance. A new treatment method may be magnetic fluid hyperthermia (MFH). Magnetoliposomes (ML), consisting of superparamagnetic iron oxide nanoparticles (SPION) stabilized with a phospholipid-bilayer, are exposed to an alternating magnetic field (AMF) to generate heat. To optimize this therapy, we investigated the effects of MFH on human PDAC cell lines and 3D organoid cultures.
MATERIAL AND METHODS: ML cytotoxicity was tested on Mia PaCa-2 and PANC-1 cells and on PDAC 3D organoid cultures, generated from resected tissue of patients. The MFH was achieved by AMF application with an amplitude of 40-47 kA/m and a frequency of 270 kHz. The MFH effect on the cell viability of the cell lines and the organoid cultures was investigated at two different time points. Clonogenic assays evaluated the impairment of colony formation. Altering ML set-ups addressed differences arising from intra- vs extracellular ML locations.
RESULTS: Mia PaCa-2 and PANC-1 cells showed no cytotoxic effects at ML concentrations up to 300 µg(Fe)/mL and 225 µg(Fe)/mL, respectively. ML at a concentration of 225 µg(Fe)/mL were also non-toxic for PDAC organoid cultures. MFH treatment using exclusively extracellular ML presented the highest impact on cell viability. Clonogenic assays demonstrated remarkable impairment as long-term outcome in MFH-treated PDAC cell lines. Additionally, we successfully treated PDAC organoids with extracellular ML-derived MFH, resulting in notably reduced cell viabilities 2h and 24 h post treatment. Still, PDAC organoids seem to partly recover from MFH after 24 h as opposed to conventional 2D-cultures.
CONCLUSION: Treatment with MFH strongly diminished pancreatic cancer cell viability in vitro, making it a promising treatment strategy. As organoids resemble the more advanced in vivo conditions better than conventional 2D cell lines, our organoid model holds great potential for further investigations.
© 2021 Palzer et al.

Entities:  

Keywords:  PDAC; SPION; magnetic fluid hyperthermia; magnetic nanoparticles; organoids; pancreatic cancer

Mesh:

Year:  2021        PMID: 33935496      PMCID: PMC8079353          DOI: 10.2147/IJN.S288379

Source DB:  PubMed          Journal:  Int J Nanomedicine        ISSN: 1176-9114


  69 in total

1.  Anticancer effect and feasibility study of hyperthermia treatment of pancreatic cancer using magnetic nanoparticles.

Authors:  Lufang Wang; Jian Dong; Weiwei Ouyang; Xiaowen Wang; Jintian Tang
Journal:  Oncol Rep       Date:  2011-11-30       Impact factor: 3.906

2.  Cytotoxic effects of iron oxide nanoparticles and implications for safety in cell labelling.

Authors:  Stefaan J H Soenen; Uwe Himmelreich; Nele Nuytten; Marcel De Cuyper
Journal:  Biomaterials       Date:  2010-09-22       Impact factor: 12.479

3.  Evaluation of magnetic nanoparticles coated by 5-fluorouracil imprinted polymer for controlled drug delivery in mouse breast cancer model.

Authors:  Hamid Hashemi-Moghaddam; Saeed Kazemi-Bagsangani; Mahdi Jamili; Saeed Zavareh
Journal:  Int J Pharm       Date:  2015-12-02       Impact factor: 5.875

4.  Treatment outcomes of concurrent hyperthermia and chemoradiotherapy for pancreatic cancer: Insights into the significance of hyperthermia treatment.

Authors:  Toshiya Maebayashi; Naoya Ishibashi; Takuya Aizawa; Masakuni Sakaguchi; Tsutomu Sato; Jiro Kawamori; Yoshiaki Tanaka
Journal:  Oncol Lett       Date:  2017-04-21       Impact factor: 2.967

Review 5.  Nanoparticle-mediated thermal therapy: evolving strategies for prostate cancer therapy.

Authors:  Sunil Krishnan; Parmeswaran Diagaradjane; Sang Hyun Cho
Journal:  Int J Hyperthermia       Date:  2010-09-21       Impact factor: 3.914

6.  Cellular uptake of magnetic fluid particles and their effects on human adenocarcinoma cells exposed to AC magnetic fields in vitro.

Authors:  A Jordan; P Wust; R Scholz; B Tesche; H Fähling; T Mitrovics; T Vogl; J Cervós-Navarro; R Felix
Journal:  Int J Hyperthermia       Date:  1996 Nov-Dec       Impact factor: 3.914

Review 7.  Basic principles of thermal dosimetry and thermal thresholds for tissue damage from hyperthermia.

Authors:  M W Dewhirst; B L Viglianti; M Lora-Michiels; M Hanson; P J Hoopes
Journal:  Int J Hyperthermia       Date:  2003 May-Jun       Impact factor: 3.914

8.  Anti-cancer effect of hyperthermia on breast cancer by magnetite nanoparticle-loaded anti-HER2 immunoliposomes.

Authors:  Toyone Kikumori; Takeshi Kobayashi; Masataka Sawaki; Tsuneo Imai
Journal:  Breast Cancer Res Treat       Date:  2008-03-02       Impact factor: 4.872

9.  Effect of heat therapy using magnetic nanoparticles conjugated with cationic liposomes on prostate tumor in bone.

Authors:  Noriyasu Kawai; Mitsuru Futakuchi; Tatsuro Yoshida; Akira Ito; Shinya Sato; Taku Naiki; Hiroyuki Honda; Tomoyuki Shirai; Kenjiro Kohri
Journal:  Prostate       Date:  2008-05-15       Impact factor: 4.104

10.  Generation and initial characterization of novel tumour organoid models to study human pancreatic cancer-induced cachexia.

Authors:  Rianne D W Vaes; David P J van Dijk; Tessa T J Welbers; Marinus J Blok; Merel R Aberle; Lara Heij; Sylvia F Boj; Steven W M Olde Damink; Sander S Rensen
Journal:  J Cachexia Sarcopenia Muscle       Date:  2020-10-13       Impact factor: 12.910

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  1 in total

Review 1.  Magnetite Nanoparticles in Magnetic Hyperthermia and Cancer Therapies: Challenges and Perspectives.

Authors:  Agnieszka Włodarczyk; Szymon Gorgoń; Adrian Radoń; Karolina Bajdak-Rusinek
Journal:  Nanomaterials (Basel)       Date:  2022-05-25       Impact factor: 5.719

  1 in total

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